vulnificus (12), and V. parahaemolyticus (13), can use heme and hemoglobin other than ferrisiderophore as iron sources, R428 cell line utilization of heme and hemoglobin by V. mimicus has been unexplored so far.

In this study, it was found that V. mimicus is able to use heme and hemoglobin, and a gene (named mhuA for V. mimicus heme utilization) encoding the heme/hemoglobin receptor was identified and characterized. It was also found that a directly upstream gene (mhuB) located in a reverse orientation to mhuA is involved in the activation of the mhuA transcription. The strains and plasmids employed in this study are listed in Table 1. Bacteria were cultured at 37oC in LB medium or LB agar containing 0.5% NaCl. Escherichia coliβ2155, a DAP auxotroph, was cultured in LB medium containing DAP at 0.5 mM. Appropriate antibiotics were added to the media at the following concentrations: ampicillin at 50 μg/ml, chloramphenicol at 10 μg/ml, and tetracycline at 10 μg/ml. To impose iron limitation on the bacteria, either EDDA (Sigma, St. Louis, MO, USA) or DPD (Wako, Osaka, Japan) was added to LB medium at a final concentration of 200 μM. Thereafter, LB media with and without either EDDA

or DPD were designated −Fe and +Fe, respectively. As needed, either bovine hemin (Sigma) or human hemoglobin (Sigma) was supplemented to the −Fe medium at 10 μM or 2.5 μM, respectively. Growth assay was carried out with a biophotorecorder TVS062CA (Advantec, Tokyo, Japan). In brief, an aliquot of overnight culture of V. mimicus grown in LB medium was inoculated at a final

OD600 of Rapamycin clinical trial 0.005 into the −Fe medium (with EDDA), to which either hemin or hemoglobin was added at a concentration as indicated above. Cultures were then shaken (70 rpm) at 37oC and the OD600 was measured every hour for 16 hr. Standard DNA manipulations were performed according to the procedures of Sambrook et al. (20). Chromosomal DNA and plasmid DNA were Myosin extracted with a Wizard genomic DNA purification kit (Promega, Madison, WI, USA) and a high pure plasmid isolation kit (Roche, Basel, Switzerland), respectively. Restriction enzymes and a DNA ligation kit were purchased from Roche or Takara (Shiga, Japan). DNA fragments from agarose gels or in sample solutions treated with restriction enzymes were purified with a MagExtractor DNA fragment purification kit (Toyobo, Osaka, Japan). Transformation of E. coli H1717 cells was carried out by electroporation with a MicroPulser apparatus (Bio-Rad, Benicia, CA, USA). Oligonucleotide primers designed according to the determined sequences of V. mimicus 7PT were used for PCR, RT-qPCR, and primer extension. To gain Fur box-containing gene fragments, FURTA (14) was performed in V. mimicus 7PT, as previously described (10, 21). These techniques were performed according to the DIG application manual for filter hybridization (Roche).